williams syndrome baby - Axtarish в Google
Williams syndrome is a disorder that causes developmental delays, learning problems (like trouble with space and numbers), and heart and blood vessel problems . But kids who have it usually have good verbal skills, are friendly and social, and may enjoy music-related activities.
Williams syndrome is a rare genetic condition characterized by unique physical features, delays in cognitive development and potential cardiovascular problems.
Symptoms. Symptoms of Williams syndrome are: Feeding problems, including colic, reflux, and vomiting. Inward bend of the small finger.
Williams syndrome is a rare developmental disorder that can affect the heart and blood vessels. Learn more from Boston Children's Hospital.
22 сент. 2024 г. · Babies with Williams syndrome are born without a section of chromosome 7 that contains between 25 and 27 genes. The symptoms your child will ...
14 окт. 2024 г. · Williams syndrome is a genetic disorder. Children have distinctive facial features and developmental delay.
31 мая 2022 г. · Young children with Williams syndrome have distinctive facial features including a broad forehead, puffiness around the eyes, a flat bridge of ...
About one in every 20,000 babies is born with Williams syndrome. Males and females are equally affected, and the condition is found across all races and ...
Most patients with Williams syndrome are diagnosed as a newborn or in early childhood. The average age of diagnosis is around three and a half years. Not all ...
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